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Details

Stereochemistry ABSOLUTE
Molecular Formula C36H28N6O10
Molecular Weight 704.6417
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLUNICATE

SMILES

O=C(N[C@H]1[C@H](OC(=O)C2=CC=CN=C2)O[C@H](COC(=O)C3=CC=CN=C3)[C@@H](OC(=O)C4=CC=CN=C4)[C@@H]1OC(=O)C5=CC=CN=C5)C6=CC=CN=C6

InChI

InChIKey=ZLNMZWDQJJAEAM-QPBDZWBWSA-N
InChI=1S/C36H28N6O10/c43-31(22-6-1-11-37-16-22)42-28-30(51-34(46)25-9-4-14-40-19-25)29(50-33(45)24-8-3-13-39-18-24)27(21-48-32(44)23-7-2-12-38-17-23)49-36(28)52-35(47)26-10-5-15-41-20-26/h1-20,27-30,36H,21H2,(H,42,43)/t27-,28-,29-,30-,36+/m1/s1

HIDE SMILES / InChI

Molecular Formula C36H28N6O10
Molecular Weight 704.6417
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Glunicate (LG 13979) is a long-acting nicotinic acid derivative that can lower plasma triglyceride levels, while leaving other lipoprotein parameters unaffected. It exerts a dose‐dependent reduction of plasma triglycerides and cholesterol. In rabbits, glunicate provided dose-dependent protection of the arterial wall from atheromatous lesions and from cholesterol and collagen accumulation. It has been shown that glunicate has prolonged activity on plasma free fatty acids and triglycerides, with long lasting and intense activity on plasma cholesterol.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:45 GMT 2023
Edited
by admin
on Fri Dec 15 16:08:45 GMT 2023
Record UNII
C62ZH19B0L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLUNICATE
INN   MART.  
INN  
Official Name English
glunicate [INN]
Common Name English
2-DEOXY-2-NICOTINAMIDO-.BETA.-D-GLUCOPYRANOSE 1,3,4,6-TETRANICOTINATE
Common Name English
GLUNICATE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C98151
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
Code System Code Type Description
SMS_ID
100000084209
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
FDA UNII
C62ZH19B0L
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
EVMPD
SUB07942MIG
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106431
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID201001487
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
NCI_THESAURUS
C87632
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
CAS
80763-86-6
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
PUBCHEM
6917785
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
INN
5483
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
MESH
C038986
Created by admin on Fri Dec 15 16:08:45 GMT 2023 , Edited by admin on Fri Dec 15 16:08:45 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY